HIV-1 infection depletes human CD34+CD38- hematopoietic progenitor cells via pDC-dependent mechanisms

被引:32
作者
Li, Guangming [1 ]
Zhao, Juanjuan [2 ]
Cheng, Liang [1 ]
Jiang, Qi
Kan, Sheng [2 ]
Qin, Enqiang [3 ]
Tu, Bo [3 ]
Zhang, Xin [3 ]
Zhang, Liguo [4 ]
Su, Lishan [1 ,4 ]
Zhang, Zheng [1 ,2 ]
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[2] Beijing 302 Hosp, Res Ctr Clin & Translat Med, Beijing, Peoples R China
[3] Beijing 302 Hosp, Treatment & Res Ctr Infect Dis, Beijing, Peoples R China
[4] Chinese Acad Sci, Inst Biophys, Key Lab Infect & Immun, Beijing, Peoples R China
基金
美国国家卫生研究院;
关键词
IMMUNODEFICIENCY-VIRUS-INFECTION; MICE IN-VIVO; PLASMACYTOID DENDRITIC CELLS; PERSISTENT LCMV INFECTION; STEM-CELLS; BONE-MARROW; ANTIRETROVIRAL THERAPY; PERIPHERAL-BLOOD; SELF-RENEWAL; IFN-GAMMA;
D O I
10.1371/journal.ppat.1006505
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chronic human immunodeficiency virus-1 (HIV-1) infection in patients leads to multilineage hematopoietic abnormalities or pancytopenia. The deficiency in hematopoietic progenitor cells (HPCs) induced by HIV-1 infection has been proposed, but the relevant mechanisms are poorly understood. We report here that both human CD34(+)CD38(-) early and CD34(+)CD38(+) intermediate HPCs were maintained in the bone marrow (BM) of humanized mice. Chronic HIV-1 infection preferentially depleted CD34(+)CD38(-) early HPCs in the BM and reduced their proliferation potential in vivo in both HIV-1-infected patients and humanized mice, while CD34(+)CD38(+) intermediate HSCs were relatively unaffected. Strikingly, depletion of plasmacytoid dendritic cells (pDCs) prevented human CD34(+)CD38(-) early HPCs from HIV-1 infection-induced depletion and functional impairment and restored the gene expression profile of purified CD34(+) HPCs in humanized mice. These findings suggest that pDCs contribute to the early hematopoietic suppression induced by chronic HIV-1 infection and provide a novel therapeutic target for the hematopoiesis suppression in HIV-1 patients.
引用
收藏
页数:20
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